Synergists to aerosol insecticides



Patented Apr. 4, 1944 UNITED STATES PATENT OFFICE SYNER-GISTS T AEROSOL INSECTICIDES William N. Sullivan, Washington, D. C., and Lyle D. Goodhue, Bcrwyn, Md., assignors to the United States oi America as represented by Claude R. Wickard, Secretary of Agriculture, and his successors in office No Drawing. Original app ication September 30,

1941, Serial No. 412,960.

Divided and this application January 7, 1944, Serial No. 517,370

(Granted under the act of March 3, 1883, as amended April 30, 1928; 370 0. G. 757) 3 Claims.

States of America for governmental purposes without the payment to us of any royalty thereon.

This is a division of our copending application for patent, Serial No. 412,960, filed September 30, 1941.

Our invention relates to materials which will increase the effectiveness of insecticides in aerosol form.

Certain agents which may or may not be toxic in themselves when added to aerosol insecticides greatly increase the rate of mortality. The increased toxicity obtained by the combination of such materials is often referred to as synergism" and the added material a synergist. Therefore, in these terms, the general object of our invention is the provision of materials suitab as synergists for aerosol insecticides.

Another object of our invention is the provision of agents which will not only increase the insecticidal action of materials known to possess some toxicity, but which will also impartinsecticidal properties to materials which are known to be non-toxic or to have a very low toxicity.

A further object of our invention is the provision of such agents acting as synergists, which can be applied by dispersion simultaneously with and by the same methods used for the preparation of aerosol insecticides.

We have found that materials suitable for the purposes of this invention belong most frequently to the class of chemical compounds which are surface active in non-aqueous solvents or which act as detergents in non-aqueous solvents. These compounds, in general, contain polar groupings such as the hydroxyl, the carboxyl, the amine, the ammonium, or the sulfonic acid, alone, in multiple, or in combination, which is attached to some long chain aliphatic radical. or, in some cases, an aromatic radical.

Substances acting as detergents or Surface active agents in non-aqueous media can be easily applied by the usual methods of aerosol production, but this invention is not limited to these substances becaus difierent methods of aerosol production can be used with different types of synergists. In this class of chemical compounds we have found the fatty acids, the mono'esters of fatty acids and ethylene or propylene glycol, of glycerine 0r sorbitol, to be especially suitable as well as fatty acids in combination with amines such as methanolamine, sulfonated aryl and alkyl radicals alone or combined with an amine.

There are manyprocesses which can be used to apply these materials in the form of aerosols, such as spraying into the atmosphere, vaporization, by chemical reaction, by spraying on a heated surface, and so forth. Although this invention is not limited to any particular method of application, our preferred method of application comprises dissolving the synergist in the insecticide, if the insecticide is a liquid, or dissolving in some solvent common to both if a solid, and spraying the solution on a heated surface, whereby an aerosol is formed composed of both the synergist and the insecticide.

A synergist to an insecticide in aerosol form is not necessarily also a synergist to an insecticide in spray form, even of the same compound. Actual tests have disclosed that an agent which possesses little or no effect as a synergist to an insecticidal spray may be extremely effective as a synergist to an insecticidal aerosol. The rea son for this it not apparent, but it would seem that the mere wetting of the insect cannot explain the action.

The following results were obtained using synergists in accordance with this invention. These results were obtained on the basis of preliminary tests first carried out in a small chamber of 7 cu. ft. and then on a larger scale in a 216 cu. ft. chamber. In each test from 500 to 600 flies were used. Six-tenths of a pound of odichlorobenzene per 1000 cu. ft. gave only a 2% kill. However, when mixed with 0.16 lb. of oleic acid as a synergist, a kill was obtained. This same quantity of oleic acid, when used alone under the same conditions gave only a 1% kill. Lauric acid when used alone in the same amount, namely, 0.16 lb. per 1000 cu. it, gave only a 1% kill, but when used as a synergist with 0.6 lb. of o-dichlorobenzene per 1000 cu. ft. a kill was obtained.

The same synergists were tested at other concentrations and it was found that little is gained by adding more than The following is a list of substances which were tested as synergists at a concentration of 0.06 lb. in 0.6 lb. of o-dichlorobenzene per 1000 cu. it. against the housefly, the percentage of kill in each case being indicated in the right hand column:

Per cent kill Spermaceti 3'7 Diglycol laurate 48 Sulfonated naphthalene 60 Salicylic acid 91 Propylene glycol oleate 28 Myristic acid 49 Propylene glycol laurate '74 Sorbitol laurate 59 v Monoglycol laurate 56 Triethanolamine oleate 56 Lauryl sulfate '10 oleic acid was effective, lauric acid was also found to be effective and vice versa. The kill without a synergist was always less than 100% and usually less than 50%.

In a 1100 cu. ft. room, naturally infested with cockroaches, more than 5000 were killed in 18 hours and none were found living, using 1 lbs. of o-dichlorobenzene with 3% lauric acid and 2% oleic acid. Excellent results were also obtained in a 3200 cu. ft. room.

Tests were also conducted against the carpet beetle larva, the confused flour beetles and crickets. The halogenated esters in combination with any one of the synergists mentioned above are extremely toxic to the confused flour beetle and produce a high mortality to the carpet beetle larva.

Among compounds tested against the housefly in the form of aerosols, in combination with synergists of the type mentioned above, are 3- chloroacenaphthene, 2-chlorofluorene, 3-chlorodibenzofuran, chlorinated diphenyls, halogenated naphthalenes, halogenated esters, halogenated ketones, carbazole, thiocresol and halogenated phenols. The synergist was shown to be responsible in each case for an increase in toxicity.

Having thus described our claim:

1. An insecticide in aerosol form comprising thiocresol and an agent chosen from the group consisting of diglycol laurate, propylene glycol oleate, propylene glycol laurate, sorbitol laurate, and monoglycol laurate.

2. An insecticide in aerosol form comprising thiocresol and lauryl sulfate.

3. An insecticide in aerosol form comprising thiocresol and sulfonated naphthalene.

invention, we

WILLIAM N. SULLIVAN. LYLE D. GOODHUE. 

